RU2017122014A - Антитела к c10orf54 и их применения - Google Patents
Антитела к c10orf54 и их применения Download PDFInfo
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- RU2017122014A RU2017122014A RU2017122014A RU2017122014A RU2017122014A RU 2017122014 A RU2017122014 A RU 2017122014A RU 2017122014 A RU2017122014 A RU 2017122014A RU 2017122014 A RU2017122014 A RU 2017122014A RU 2017122014 A RU2017122014 A RU 2017122014A
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- 238000000034 method Methods 0.000 claims 12
- 210000004027 cell Anatomy 0.000 claims 7
- 239000012634 fragment Substances 0.000 claims 7
- 206010028980 Neoplasm Diseases 0.000 claims 6
- 201000011510 cancer Diseases 0.000 claims 6
- 108091058539 C10orf54 Proteins 0.000 claims 5
- 102100038282 V-type immunoglobulin domain-containing suppressor of T-cell activation Human genes 0.000 claims 5
- 125000003275 alpha amino acid group Chemical group 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 239000000611 antibody drug conjugate Substances 0.000 claims 3
- 229940049595 antibody-drug conjugate Drugs 0.000 claims 3
- 108090000623 proteins and genes Proteins 0.000 claims 3
- 210000004881 tumor cell Anatomy 0.000 claims 3
- 210000001744 T-lymphocyte Anatomy 0.000 claims 2
- 239000000427 antigen Substances 0.000 claims 2
- 102000036639 antigens Human genes 0.000 claims 2
- 108091007433 antigens Proteins 0.000 claims 2
- 230000002708 enhancing effect Effects 0.000 claims 2
- 239000013604 expression vector Substances 0.000 claims 2
- 102000037865 fusion proteins Human genes 0.000 claims 2
- 108020001507 fusion proteins Proteins 0.000 claims 2
- 230000002998 immunogenetic effect Effects 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 239000002157 polynucleotide Substances 0.000 claims 2
- 102000040430 polynucleotide Human genes 0.000 claims 2
- 108091033319 polynucleotide Proteins 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 208000024891 symptom Diseases 0.000 claims 2
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 208000017897 Carcinoma of esophagus Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims 1
- 201000008808 Fibrosarcoma Diseases 0.000 claims 1
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 claims 1
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 208000008839 Kidney Neoplasms Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 108700026244 Open Reading Frames Proteins 0.000 claims 1
- 206010038389 Renal cancer Diseases 0.000 claims 1
- 208000000453 Skin Neoplasms Diseases 0.000 claims 1
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 102100031083 Uteroglobin Human genes 0.000 claims 1
- 108090000203 Uteroglobin Proteins 0.000 claims 1
- 230000004913 activation Effects 0.000 claims 1
- 229940125644 antibody drug Drugs 0.000 claims 1
- 210000000349 chromosome Anatomy 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 239000000562 conjugate Substances 0.000 claims 1
- 238000012258 culturing Methods 0.000 claims 1
- 230000016396 cytokine production Effects 0.000 claims 1
- 229940127089 cytotoxic agent Drugs 0.000 claims 1
- 239000002254 cytotoxic agent Substances 0.000 claims 1
- 231100000599 cytotoxic agent Toxicity 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 206010017758 gastric cancer Diseases 0.000 claims 1
- 230000012010 growth Effects 0.000 claims 1
- 230000028993 immune response Effects 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 201000010982 kidney cancer Diseases 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 208000014018 liver neoplasm Diseases 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000002773 nucleotide Substances 0.000 claims 1
- 125000003729 nucleotide group Chemical group 0.000 claims 1
- 210000000496 pancreas Anatomy 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000035755 proliferation Effects 0.000 claims 1
- 210000003289 regulatory T cell Anatomy 0.000 claims 1
- 201000000849 skin cancer Diseases 0.000 claims 1
- 201000011549 stomach cancer Diseases 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 230000004614 tumor growth Effects 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
Classifications
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
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- A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
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- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
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- A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
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- A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
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- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2827—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/577—Immunoassay; Biospecific binding assay; Materials therefor involving monoclonal antibodies binding reaction mechanisms characterised by the use of monoclonal antibodies; monoclonal antibodies per se are classified with their corresponding antigens
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- A—HUMAN NECESSITIES
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- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/567—Framework region [FR]
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
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- C07—ORGANIC CHEMISTRY
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- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/74—Inducing cell proliferation
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
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- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70503—Immunoglobulin superfamily, e.g. VCAMs, PECAM, LFA-3
- G01N2333/70532—B7 molecules, e.g. CD80, CD86
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Claims (63)
1. Выделенное антитело или его антигенсвязывающий фрагмент, которое(ый) связывается с первой группой белков или химерных белков C10orf54 (белков, кодируемых геном из открытой рамки считывания 54 на хромосоме 10), обозначенных как СС1 (SEQ ID NO: 1079), СС4 (SEQ ID NO: 1245), CC5 (SEQ ID NO: 1246), CC8 (SEQ ID NO: 1249) и CC10 (SEQ ID NO: 1251), и не связывается со второй группой белков или химерных белков C10orf54, обозначенных как СС2 (SEQ ID NO: 1243), СС3 (SEQ ID NO: 1244), CC6 (SEQ ID NO: 1247), CC7 (SEQ ID NO: 1248) и CC9 (SEQ ID NO: 1250).
2. Антитело по п. 1 или его антигенсвязывающий фрагмент, где указанное антитело представляет собой моноклональное антитело.
3. Антитело по любому из пп. 1 или 2 или его антигенсвязывающий фрагмент, где указанное антитело выбрано из группы, состоящей из:
(a) антитела 5В, содержащего:
- тяжелую цепь (Н), содержащую следующие три CDR (определяющих комплементарность участка), которые определены согласно IMGT (ImMunoGeneTics; база данных по иммуногенетике), соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1292, CDR-H2, имеющий последовательность с SEQ ID NO: 1337, и CDR-H3, имеющий последовательность с SEQ ID NO: 1386; и
- легкую цепь (L), содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1426, CDR-L2, имеющий последовательность с SEQ ID NO: 1474, и CDR-L3, имеющий последовательность с SEQ ID NO: 1493;
(b) антитела 46А, содержащего:
тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1292, CDR-H2, имеющий последовательность с SEQ ID NO: 1342, и CDR-H3, имеющий последовательность с SEQ ID NO: 1390; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1426, CDR-L2, имеющий последовательность с SEQ ID NO: 1474, и CDR-L3, имеющий последовательность с SEQ ID NO: 1496;
(c) антитела 128А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1292, CDR-H2, имеющий последовательность с SEQ ID NO: 1337, и CDR-H3, имеющий последовательность с SEQ ID NO: 1386; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1426, CDR-L2, имеющий последовательность с SEQ ID NO: 1474, и CDR-L3, имеющий последовательность с SEQ ID NO: 1493;
(d) антитела 146С, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1292, CDR-H2, имеющий последовательность с SEQ ID NO: 1337, и CDR-H3, имеющий последовательность с SEQ ID NO: 1386; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1426, CDR-L2, имеющий последовательность с SEQ ID NO: 1474, и CDR-L3, имеющий последовательность с SEQ ID NO: 1493;
(e) антитела 208А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1292, CDR-H2, имеющий последовательность с SEQ ID NO: 1337, и CDR-H3, имеющий последовательность с SEQ ID NO: 1386; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1426, CDR-L2, имеющий последовательность с SEQ ID NO: 1474, и CDR-L3, имеющий последовательность с SEQ ID NO: 1493;
(f) антитела 26А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1297, CDR-H2, имеющий последовательность с SEQ ID NO: 1355, и CDR-H3, имеющий последовательность с SEQ ID NO: 1394; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1432, CDR-L2, имеющий последовательность с SEQ ID NO: 1477, и CDR-L3, имеющий последовательность с SEQ ID NO: 1499;
(g) антитела 164А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1099, CDR-H2, имеющий последовательность с SEQ ID NO: 1360, и CDR-H3, имеющий последовательность с SEQ ID NO: 1398; и
- легкую цепь, содержащую:
(h) антитела 230А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1302, CDR-H2, имеющий последовательность с SEQ ID NO: 1365, и CDR-H3, имеющий последовательность с SEQ ID NO: 1402; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1455, CDR-L2, имеющий
последовательность с SEQ ID NO: 1103, и CDR-L3, имеющий последовательность с SEQ ID NO: 1505;
(i) антитела 33А, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1312, CDR-H2, имеющий последовательность с SEQ ID NO: 1082, и CDR-H3, имеющий последовательность с SEQ ID NO: 1410; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1102, CDR-L2, имеющий последовательность с SEQ ID NO: 1103, и CDR-L3, имеющий последовательность с SEQ ID NO: 1511;
(j) антитела 321D, содержащего:
- тяжелую цепь, содержащую следующие три CDR, которые определены согласно IMGT, соответственно, CDR-H1, имеющий последовательность с SEQ ID NO: 1322, CDR-H2, имеющий последовательность с SEQ ID NO: 1082, и CDR-H3, имеющий последовательность с SEQ ID NO: 1083; и
- легкую цепь, содержащую: следующие три CDR, которые определены согласно IMGT, соответственно, CDR-L1, имеющий последовательность с SEQ ID NO: 1102, CDR-L2, имеющий последовательность с SEQ ID NO: 1103, и CDR-L3, имеющий последовательность с SEQ ID NO: 1514.
4. Антитело по любому из пп. 1-3 или его антигенсвязывающий фрагмент, где указанное антитело является гуманизированным.
5. Антитело по п. 4 или его антигенсвязывающий фрагмент, причем указанное антитело выбрано из группы, состоящей из:
(а) антитела 26А, содержащего вариабельный домен тяжелой цепи с последовательностью, выбранной среди аминокислотных последовательностей с SEQ ID NO: 1529, SEQ ID NO: 1530 и SEQ ID NO: 1531, и вариабельный домен легкой цепи с последовательностью, выбранной среди аминокислотных последовательностей с SEQ ID NO: 1532, SEQ ID NO: 1533 и SEQ ID NO: 1534;
(b) антитела 128A, содержащего вариабельный домен тяжелой цепи с последовательностью, выбранной среди аминокислотных последовательностей с SEQ ID NO: 1535, SEQ ID NO: 1536 и SEQ ID NO: 1537, и вариабельный домен легкой цепи с последовательностью, выбранной среди аминокислотных последовательностей с SEQ ID NO: 1538, SEQ ID NO: 1539 и SEQ ID NO: 1540.
6. Антитело по любому из пп. 1-5, где антитело представляет собой Fab фрагмент, F(ab')2 фрагмент, одноцепочечный Fv (sFv), диатело, триотело или миниантитело.
7. Конъюгат антитело-лекарственное средство, содержащий антитело по любому из пп. 1-6, конъюгированное с цитотоксическим агентом.
8. Полинуклеотид, содержащий нуклеотидную последовательность, кодирующую антитело по любому из пп. 1-6.
9. Экспрессирующий вектор, содержащий полинуклеотид по п. 8.
10. Клетка-хозяин, содержащая экспрессирующий вектор по п. 9.
11. Способ получения антитела или его антигенсвязывающего фрагмента по любому из пп. 1-6, включающий стадию культивирования клетки хозяина по п. 10 в условиях, которые способствуют продуцированию данного антитела.
12. Фармацевтическая композиция, содержащая антитело по любому из пп. 1-6 или конъюгат антитело-лекарственное средство по п. 7 и фармацевтически приемлемый разбавитель, носитель или эксципиент.
13. Способ лечения, предупреждения или облегчения одного или более симптомов рака, включающий введение субъекту терапевтически эффективного количества композиции по п. 12, в результате чего осуществляется лечение, предупреждение или облегчение одного или более симптомов рака.
14. Способ по п. 13, где рак представляет собой лейкоз, предпочтительно острый миелоидный лейкоз (AML), рак мочевого пузыря, рак кожи, рак толстой кишки, рак молочной железы, рак печени, рак почки, рак легкого, рак желудка, рак поджелудочной железы, рак пищевода или фибросаркому.
15. Способ ингибирования роста опухоли с воспалением у субъекта, включающий введение субъекту эффективного количества композиции по п. 12.
16. Способ ингибирования роста клетки, экспрессирующей C10orf54 на своей поверхности, включающий приведение в контакт данной клетки с эффективным количеством композиции по п. 12.
17. Способ по п. 16, где клетка представляет собой регуляторную Т-клетку.
18. Способ по п. любому из пп. 16 или 17, где данная клетка представляет собой раковую или предраковую клетку.
19. Способ модулирования иммунного ответа у субъекта, включающий введение субъекту эффективного количества композиции по п. 12.
20. Способ по п. 19, где модулирование включает:
(a) усиление активации Т-клеток;
(b) усиление пролиферации Т-клеток; или
(c) усиление продуцирования цитокинов.
21. Способ лечения рака, включающий введение субъекту терапевтически эффективного количества антитела по любому из пп. 1-6 или конъюгата антитело-лекарственное средство по п. 7.
22. Способ уничтожения опухолевой клетки, включающий приведение в контакт C10orf54-экспрессирующей опухолевой клетки с количеством антитела по любому из пп. 1-6 или конъюгата антитело-лекарственное средство по п. 7, эффективным для уничтожения данной опухолевой клетки.
23. Способ детекции C10orf54 в образце, включающий приведение в контакт данного образца с антителом по любому из пп. 1-6.
24. Набор, содержащий антитело по любому из пп. 1-6.
25. Набор по п. 24, где указанное антитело конъюгировано с детектируемым субстратом.
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